Xia Fangfang, Jin Zhousheng, Dong Jiaojiao, Chen Chaoxing, Cai Yaoyao, Wang Quanguang, Chen Hongfei
Department of Anesthesiology, The First Affiliated Hospital of Wenzhou Medical University, Zhejiang, Wenzhou, China.
Evid Based Complement Alternat Med. 2022 May 11;2022:3055039. doi: 10.1155/2022/3055039. eCollection 2022.
Lung ischemia-reperfusion injury (LIRI), which has a mortality rate of approximately 50%, is a popular topic in critical care research. Keratinocyte growth factor-2 (KGF-2) is secreted by mesenchymal cells, and it is effective in promoting the proliferation, migration, and differentiation of various epithelial cells. To date, however, only a few reports on KGF-2-related regulators in LIRI have been published. In the current study, an LIRI rat model is constructed, and the upregulation of the fibroblast growth factor receptor 2 (FGFR2) is observed in the LIRI rat model. In addition, LIRI induces NLRP1 inflammasome activation in vivo and in vitro, and KGF-2 inhibits LIRI-induced damage to pulmonary microvascular endothelial cells. Mechanistically, KGF-2 inhibits NLRP1 inflammasome and NF-B activity. KGF-2 inhibition attenuates LIRI injury-induced damage to endothelial integrity. In conclusion, KGF-2 protects against LIRI by inhibiting inflammation-induced endothelial barrier damage.
肺缺血再灌注损伤(LIRI)的死亡率约为50%,是重症监护研究中的一个热门话题。角质形成细胞生长因子-2(KGF-2)由间充质细胞分泌,对促进各种上皮细胞的增殖、迁移和分化有效。然而,迄今为止,关于LIRI中与KGF-2相关的调节因子的报道很少。在本研究中,构建了LIRI大鼠模型,在该模型中观察到成纤维细胞生长因子受体2(FGFR2)上调。此外,LIRI在体内和体外均可诱导NLRP1炎性小体激活,而KGF-2可抑制LIRI诱导的肺微血管内皮细胞损伤。机制上,KGF-2抑制NLRP1炎性小体和NF-κB活性。KGF-2抑制可减轻LIRI损伤诱导的内皮完整性破坏。总之,KGF-2通过抑制炎症诱导的内皮屏障损伤来预防LIRI。